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Symbol
Name
ID
Sfxn4
sideroflexin 4
MGI:2137680
Phenotype annotations related to hematopoietic system
Darker colors indicate more annotations
Human Phenotypes
Macrocytic anemia
Hypersegmentation of neutrophil nuclei
Disease(s) Associated with SFXN4
combined oxidative phosphorylation deficiency 18

Mouse Phenotypes
decreased leukocyte cell number
Availability Mouse Genotype
Sfxn4tm1b(KOMP)Wtsi/Sfxn4tm1b(KOMP)Wtsi

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory